INTERTOCINE-S

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Informacije o zdravilu

Ime zdravila:

INTERTOCINE-S

Učinkovina:

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Ciljne živalske vrste:

govedo
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Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian
Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian
Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian
Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian
Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian

Pot uporabe:

intramuskularna uporaba
Subkutana uporaba
Intravenska uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

0.02

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

Anatomsko-terapevtsko-kemična veterinarska oznaka klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):

QN01BB02

Pravni status za dobavo/izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja za promet z zdravilom:

Surrendered

Ima dovoljenje za promet v:

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Opis ovojnine zdravila:

Na voljo samo v Greek
Na voljo samo v Greek

Dodatne informacije

Vrsta dovoljenja:

Na voljo samo v English French Croatian Italian Latvian Finnish Swedish Icelandic Norwegian

Pravna podlaga za izdajo dovoljenja za promet z zdravilom:

Na voljo samo v English Italian Latvian Lithuanian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Intervet International B.V.

Datum dovoljenja za promet z zdravilom:

20/03/1975

Proizvodna mesta, odgovorna za sproščanje serij:

Intervet International B.V.

Pristojni organ:

Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment

Številka dovoljenja za promet z zdravilom:

5256

Datum spremembe statusa dovoljenja za promet:

20/03/1975

Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet

Dokumenti

Povzetek glavnih značilnosti zdravila

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Objavljeno na dan: 11/07/2022

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